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BOC-L-2-(5-CHLOROTHIENYL)ALANINE is a chemical compound characterized by the molecular formula C14H18ClNO4S. It is a derivative of the naturally occurring amino acid alanine, featuring a 5-chlorothienyl group attached to the alpha carbon and a BOC (tert-butoxycarbonyl) protecting group on the amino group. BOC-L-2-(5-CHLOROTHIENYL)ALANINE plays a significant role in organic synthesis and peptide chemistry, serving as a building block for the creation of peptides and other bioactive molecules.

190319-94-9

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190319-94-9 Usage

Uses

Used in Organic Synthesis:
BOC-L-2-(5-CHLOROTHIENYL)ALANINE is used as a building block in organic synthesis for the construction of complex organic molecules. Its unique structure allows for the formation of various chemical bonds and reactions, contributing to the synthesis of a wide range of compounds.
Used in Peptide Chemistry:
In peptide chemistry, BOC-L-2-(5-CHLOROTHIENYL)ALANINE is utilized as a key component in the synthesis of peptides. Its incorporation into peptide sequences enables the creation of bioactive peptides with specific functions and properties.
Used in Pharmaceutical Industry:
BOC-L-2-(5-CHLOROTHIENYL)ALANINE is employed as a valuable tool in the pharmaceutical industry for the development of new drugs and biologically active compounds. Its unique chemical properties and reactivity make it suitable for the design and synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in Drug Development:
In drug development, BOC-L-2-(5-CHLOROTHIENYL)ALANINE serves as a crucial building block for the synthesis of drug candidates. Its versatility in forming different chemical entities allows researchers to explore new chemical space and identify potential drug candidates with improved pharmacological properties.
Used in Bioactive Molecule Synthesis:
BOC-L-2-(5-CHLOROTHIENYL)ALANINE is used in the synthesis of bioactive molecules, which are compounds that exhibit biological activity and have potential applications in medicine, agriculture, and other fields. Its unique structural features enable the development of molecules with specific biological targets and therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 190319-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,3,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 190319-94:
(8*1)+(7*9)+(6*0)+(5*3)+(4*1)+(3*9)+(2*9)+(1*4)=139
139 % 10 = 9
So 190319-94-9 is a valid CAS Registry Number.

190319-94-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-((tert-butoxycarbonyl)amino)-3-(5-chlorothiophen-2-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:190319-94-9 SDS

190319-94-9Downstream Products

190319-94-9Relevant academic research and scientific papers

Studies on Cyclic Dipeptides, I: Aryl Modifications of cyclo-[Phe-His]

Noe,Weigand,Pirker

, p. 1081 - 1097 (2007/10/03)

Seven new cyclic dipeptides have been synthesized and tested for their applicability as tools to elucidate the mechanism of formation of mandelonitrile with (SS)-cyclo-[Phe-His] type catalysts. Conformational analyses based on 1H NMR spectra are presented for all prepared cyclic dipeptides.

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